Mineral Chemistry, S-Pb-O Isotopes, and S/Se Ratios of the Niubiziliang Ni-(Cu) Sulfide Deposit in North Qaidam Orogenic Belt, NW China: Constraints on the Parental Magma Composition, Evolution, and Sulfur Saturation Mechanism

The Niubiziliang Ni-(Cu) deposit is the first magmatic Ni-Cu sulfide deposit in the North Qaidam Orogenic Belt (NQOB), NW China, and plays a significant role in geological evolution, Ni-Cu mineralization, and exploration in the NQOB. Here, we report on the mineral chemistry, S-Pb-O isotopes, and S/Se ratios of the mafic-ultramafic complex, which provide insights on the parental magma, evolution, and sulfur saturation mechanism. The Niubiziliang mafic-ultramafic intrusion contains four ore blocks and about ten Ni-(Cu) ore/mineralization bodies. Olivines in Niubiziliang belong to the species of chrysolite with Fo values of 88~89, and the pyroxenes are mainly orthopyroxene (En = 79~82) and clinopyroxene (En = 44~40). The olivines and some pyroxenes likely crystallized in a magma chamber at a depth of 35.45~36.55 km at a high temperature (1289~1369 °C) and pressure (9.38~9.67 kbar), whereas the Niubiziliang complex formed at a moderate depth (8.13~8.70 km) with a temperature and pressure of 1159~1253 °C and 2.15~2.30 kbar, respectively. The parental magma was considered to be high-Mg picritic basalt with MgO and NiO contents of 14.95~16.58% and 0.053~0.068%, respectively, which indicated high-degree partial melting of the depleted mantle. The mantle-derived primary magma underwent significant fractional crystallization and crustal assimilation and contamination, which was strongly supported by S-Pb-O isotope data and S/Se ratios, resulting in sulfur saturation and sulfide immiscibility in the magma. Crustal assimilation and contamination contributed more to sulfur saturation than fractional crystallization.

Transition metals in komatiitic olivine: Proxies for mantle composition, redox conditions, and sulfide mineralization potential

We present the results of a comprehensive study on the concentrations of first-row transition elements (FRTE: Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn), as well as Ga and Ge, in liquidus olivine from 2.7–3.5 Ga old Al-undepleted and Al-depleted komatiites from the Kaapvaal and Zimbabwe Cratons in southern Africa, the Yilgarn Craton in Australia, and the Superior Craton in Canada. The sample set includes komatiites that remained sulfur-undersaturated upon emplacement, as well as komatiites that reached sulfide saturation owing to assimilation of crustal sulfur.All olivine grains display concentrations of Mn, Zn, Ge, Co, Fe, Mg, and Ni similar to the Bulk Silicate Earth (BSE) values, with significant negative anomalies in Sc, Ti, V, Cr, Ga, and Cu. Olivine from the studied Al-depleted komatiites displays on average higher 100×Ga/Sc ratios (>5) than olivine from Al-undepleted komatiites (≤5). Because garnet preferentially incorporates Sc over Ga, the data suggest that elevated Ga/Sc ratios in komatiitic olivine are indicative of garnet retention in the source region of komatiites, highlighting the potential of olivine trace element chemistry as a proxy for the depth of komatiite melting and separation of the magma from the melting residue. Copper concentrations in the studied olivine grains are controlled by sulfur saturation of the host komatiite during olivine crystallization. Olivine from sulfur-undersaturated komatiite systems displays Cu concentrations mostly between 1 and 10 ppm, whereas olivine from sulfide-bearing komatiites has Cu contents of <0.5 ppm. Because komatiites contain some of the world's highest metal tenor magmatic Ni-Cu sulfide deposits, the Cu variability in olivine as a function of the sulfide-saturation state highlights a potential application of olivine chemistry in the exploration for sulfide ore deposits.Olivine from the Paleo-Archean (3.5–3.3 Ga) komatiites displays overall higher V/Sc ratios (V/Sc = 2.1 ± 0.96; 2 S.D.) than olivine from their Neo-Archean (2.7 Ga) counterparts (V/Sc = 1.0 ± 0.81, 2 S.D.). Vanadium and Sc behave similarly during partial melting of the mantle and are similarly compatible in majorite garnet. However, V is redox-sensitive and its compatibility in olivine increases as the system becomes less oxidized, whereas Sc is redox-insensitive. We argue that olivine from the studied Paleo-Archean komatiites crystallized from more reduced magmas than their Neo-Archean counterparts. Elevated Fe/Mn ratios in olivine from Paleo-Archean komatiites mimic the V/Sc signatures and are interpreted to reflect that Fe2+ is more compatible in olivine than Fe3+. These results imply that V/Sc and Fe/Mn in komatiitic olivine may potentially provide insight into the evolution of the oxidation state of the Archean mantle. Additional studies that integrate the chemistry of komatiitic olivine with those of relict interstitial glass and melt/fluid inclusions are encouraged to fully understand and quantify the potential of FRTE in olivine as a proxy for the oxidation state of the mantle sources of komatiite magmas.

Sulfide saturation mechanisms in gabbroic intrusions in the Nipigon Embayment

The Seagull and Kitto intrusions in the Nipigon Embayment of northwestern Ontario were studied to gain an understanding of the processes involved in sulfur saturation of the mafic to ultramafic magmas leading to the formation of platinum group element (PGE) concentrations. Profiles of sulfur, copper, nickel, gold, palladium, and platinum concentrations as a function of depth revealed that sulfur saturation occurred at the base of the Seagull intrusion. A higher grade horizon occurs well above the base of the intrusion, suggesting that a reef-type of process was significant here and possibly in the Kitto intrusion, as well. Olivine compositions indicate that, in both cases, the parental magmas were undersaturated with respect to sulfur. Sulfur, neodymium–samarium, and rubidium–strontium isotopic data suggest that assimilation of country rock and sulfide played a role, especially in the formation of basal concentrations of PGEs.